Variant report

Variant	nsv969396
Chromosome Location	chr6:44216621-44221180
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:36)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:44216083..44217678-chr6:44271012..44273836,2	MCF-7	breast:
2	chr6:44122736..44127198-chr6:44213713..44218106,8	K562	blood:
3	chr6:43637159..43639334-chr6:44216185..44218215,2	K562	blood:
4	chr6:44217074..44219201-chr6:44303234..44306266,3	K562	blood:
5	chr6:44099546..44105774-chr6:44219938..44225862,7	K562	blood:
6	chr6:43738049..43742352-chr6:44213795..44216744,7	K562	blood:
7	chr6:44213575..44218708-chr6:44278177..44283526,11	K562	blood:
8	chr6:44044085..44046991-chr6:44216069..44218144,2	K562	blood:
9	chr6:44040622..44046991-chr6:44213898..44218144,6	K562	blood:
10	chr6:43593505..43599096-chr6:44213646..44217999,9	K562	blood:
11	chr6:44220564..44222715-chr6:44354509..44356656,2	MCF-7	breast:
12	chr6:44216828..44218567-chr6:86441664..86443185,4	K562	blood:
13	chr6:44093312..44099146-chr6:44212809..44220233,13	MCF-7	breast:
14	chr6:44214289..44217035-chr6:44262196..44266038,3	K562	blood:
15	chr6:44187521..44192952-chr6:44212221..44217106,13	MCF-7	breast:
16	chr6:44216338..44218124-chr6:44278260..44280536,2	MCF-7	breast:
17	chr6:43610212..43612604-chr6:44219697..44221685,2	K562	blood:
18	chr4:70555494..70558474-chr6:44219167..44221609,2	K562	blood:
19	chr6:44138460..44140248-chr6:44216411..44219191,2	MCF-7	breast:
20	chr6:44215194..44217832-chr6:44265456..44268236,2	K562	blood:
21	chr6:44189603..44194222-chr6:44219459..44225598,7	MCF-7	breast:
22	chr6:44093355..44100261-chr6:44212966..44217093,13	K562	blood:
23	chr6:44213880..44217687-chr6:44354177..44357164,5	K562	blood:
24	chr6:43596077..43597604-chr6:44220846..44222458,2	K562	blood:
25	chr6:44213056..44218708-chr6:44277561..44284910,14	K562	blood:
26	chr6:44086896..44089729-chr6:44217507..44220003,2	K562	blood:
27	chr6:44218284..44220529-chr6:44245737..44248660,2	MCF-7	breast:
28	chr6:44216828..44218567-chr6:86441668..86443185,2	K562	blood:
29	chr6:43596586..43599214-chr6:44212975..44217729,5	K562	blood:
30	chr6:44119338..44121268-chr6:44217080..44219082,2	K562	blood:
31	chr17:46185336..46187355-chr6:44217982..44220067,2	MCF-7	breast:
32	chr6:44133200..44145960-chr6:44211718..44220192,28	K562	blood:
33	chr6:44147611..44150566-chr6:44216082..44217959,2	K562	blood:
34	chr6:43740852..43742547-chr6:44215186..44217318,2	K562	blood:
35	chr6:28864761..28865369-chr6:44216136..44216861,2	Hela-S3	cervix:
36	chr6:44102300..44103810-chr6:44217085..44219374,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000237686	chromatin interactions
ENSG00000137225	chromatin interactions
ENSG00000137216	chromatin interactions
ENSG00000112715	chromatin interactions
ENSG00000096401	chromatin interactions
ENSG00000112759	chromatin interactions
ENSG00000272114	chromatin interactions
ENSG00000172432	chromatin interactions
ENSG00000146221	chromatin interactions
ENSG00000124688	chromatin interactions
ENSG00000180992	chromatin interactions
ENSG00000124608	chromatin interactions
ENSG00000231881	chromatin interactions

Extended variants
information (count: 312 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:312 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561630267	chr6:44216624-44216625	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
2	rs375714759	chr6:44216666-44216667	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
3	rs34242258	chr6:44216673-44216674	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
4	rs541102211	chr6:44216690-44216691	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
5	rs532394641	chr6:44216692-44216693	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
6	rs369409889	chr6:44216693-44216694	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
7	rs559528507	chr6:44216695-44216696	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
8	rs532968757	chr6:44216714-44216715	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
9	rs540665649	chr6:44216757-44216758	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
10	rs541111236	chr6:44216789-44216790	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
11	rs551694487	chr6:44216790-44216791	Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
12	rs563433454	chr6:44216819-44216820	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
13	rs34242605	chr6:44216831-44216832	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs185732706	chr6:44216834-44216835	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
15	rs567293735	chr6:44216875-44216876	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
16	rs146602108	chr6:44216878-44216879	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
17	rs201741505	chr6:44216883-44216884	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
18	rs146444963	chr6:44216886-44216887	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
19	rs534817752	chr6:44216894-44216895	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
20	rs149113108	chr6:44216896-44216897	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
21	rs571847910	chr6:44216907-44216908	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
22	rs372589999	chr6:44216942-44216943	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
23	rs371801142	chr6:44216943-44216944	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
24	rs538852817	chr6:44216958-44216959	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
25	rs143211110	chr6:44216963-44216964	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
26	rs575861060	chr6:44217045-44217046	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
27	rs536914257	chr6:44217046-44217047	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
28	rs369825438	chr6:44217063-44217064	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
29	rs11538983	chr6:44217131-44217132	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
30	rs149441958	chr6:44217134-44217135	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
31	rs147535516	chr6:44217150-44217151	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
32	rs138497879	chr6:44217160-44217161	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
33	rs11538982	chr6:44217197-44217198	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
34	rs143977102	chr6:44217200-44217201	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
35	rs373969944	chr6:44217206-44217207	Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
36	rs201634463	chr6:44217209-44217210	Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
37	rs61753592	chr6:44217210-44217211	Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
38	rs11538987	chr6:44217216-44217217	Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
39	rs372668329	chr6:44217225-44217226	Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs552784311	chr6:44217251-44217252	Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
41	rs147289632	chr6:44217258-44217259	Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
42	rs201247226	chr6:44217277-44217278	Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
43	rs375952776	chr6:44217351-44217352	Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
44	rs370884816	chr6:44217359-44217360	Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
45	rs34083426	chr6:44217374-44217375	Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs563463594	chr6:44217375-44217376	Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
47	rs530733445	chr6:44217392-44217393	Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
48	rs187823187	chr6:44217404-44217405	Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
49	rs142538541	chr6:44217465-44217466	Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs113937534	chr6:44217480-44217481	Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Colorectal cancer	16790693	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Systemic lupus erythematosus	19287148	CNVD
Colorectal cancer	19359472	CNVD
Multiple myeloma	16616336	CNVD
Chordoma	18071362	CNVD
Follicular lymphoma	16790693	CNVD
Osteosarcoma	19286668	CNVD
Neurocytoma	17123091	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	21569311	CNVD
Cancer	20164920	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:360 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44213600-44217000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:44214000-44216800	Active TSS	Pancreas	Pancrea
3	chr6:44214000-44217000	Active TSS	HSMMtube	muscle
4	chr6:44214200-44217800	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
5	chr6:44214800-44220200	Transcr. at gene 5' and 3'	Pancreatic Islets	Pancreatic Islet
6	chr6:44215000-44220000	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
7	chr6:44215400-44216800	Transcr. at gene 5' and 3'	Fetal Stomach	stomach
8	chr6:44215400-44217800	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr6:44215400-44218400	Transcr. at gene 5' and 3'	Dnd41	blood
10	chr6:44215400-44218600	Transcr. at gene 5' and 3'	A549	lung
11	chr6:44215600-44217000	Transcr. at gene 5' and 3'	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr6:44215600-44217000	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
13	chr6:44215600-44217200	Transcr. at gene 5' and 3'	H9 Cell Line	embryonic stem cell
14	chr6:44215600-44217200	Transcr. at gene 5' and 3'	Brain Hippocampus Middle	brain
15	chr6:44215600-44217400	Transcr. at gene 5' and 3'	HUES6 Cell Line	embryonic stem cell
16	chr6:44215600-44217400	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
17	chr6:44215600-44217600	Transcr. at gene 5' and 3'	H1 Cell Line	embryonic stem cell
18	chr6:44215600-44217600	Transcr. at gene 5' and 3'	NHEK	skin
19	chr6:44215600-44217800	Transcr. at gene 5' and 3'	HUES64 Cell Line	embryonic stem cell
20	chr6:44215600-44218400	Transcr. at gene 5' and 3'	iPS-20b Cell Line	embryonic stem cell
21	chr6:44215800-44216800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr6:44215800-44216800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr6:44215800-44217000	Active TSS	Right Atrium	heart
24	chr6:44215800-44217200	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr6:44215800-44217200	Transcr. at gene 5' and 3'	Fetal Adrenal Gland	Adrenal Gland
26	chr6:44215800-44217200	Transcr. at gene 5' and 3'	HSMM	muscle
27	chr6:44215800-44217400	Transcr. at gene 5' and 3'	iPS-18 Cell Line	embryonic stem cell
28	chr6:44215800-44217400	Transcr. at gene 5' and 3'	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr6:44215800-44217600	Transcr. at gene 5' and 3'	HUES48 Cell Line	embryonic stem cell
30	chr6:44215800-44217600	Transcr. at gene 5' and 3'	K562	blood
31	chr6:44215800-44217800	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr6:44215800-44217800	Transcr. at gene 5' and 3'	HMEC	breast
33	chr6:44215800-44218400	Transcr. at gene 5' and 3'	HUVEC	blood vessel
34	chr6:44215800-44218800	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr6:44215800-44218800	Transcr. at gene 5' and 3'	Hela-S3	cervix
36	chr6:44215800-44221400	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
37	chr6:44216000-44216800	Transcr. at gene 5' and 3'	ES-I3 Cell Line	embryonic stem cell
38	chr6:44216000-44216800	Transcr. at gene 5' and 3'	Fetal Intestine Large	intestine
39	chr6:44216000-44216800	Weak transcription	Gastric	stomach
40	chr6:44216000-44217000	Transcr. at gene 5' and 3'	NHDF-Ad	bronchial
41	chr6:44216000-44217200	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells	blood
42	chr6:44216000-44217400	Transcr. at gene 5' and 3'	Brain Cingulate Gyrus	brain
43	chr6:44216000-44217600	Transcr. at gene 5' and 3'	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr6:44216000-44217600	Transcr. at gene 5' and 3'	Muscle Satellite Cultured Cells	--
45	chr6:44216000-44217600	Transcr. at gene 5' and 3'	Brain Anterior Caudate	brain
46	chr6:44216000-44217600	Transcr. at gene 5' and 3'	Brain Substantia Nigra	brain
47	chr6:44216000-44217600	Transcr. at gene 5' and 3'	NH-A	brain
48	chr6:44216200-44216800	Transcr. at gene 5' and 3'	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr6:44216200-44216800	Transcr. at gene 5' and 3'	Fetal Muscle Trunk	muscle
50	chr6:44216200-44217200	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood

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