Variant report

Variant	esv3421071
Chromosome Location	chr6:34110799-34113347
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:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:34111438..34113496-chr6:34384142..34385841,2	MCF-7	breast:
2	chr6:34110331..34113788-chr6:34116260..34119382,3	MCF-7	breast:
3	chr6:34023119..34023631-chr6:34111504..34112235,2	K562	blood:
4	chr6:34023070..34025324-chr6:34112183..34113758,2	MCF-7	breast:
5	chr6:34096880..34099579-chr6:34108497..34110851,2	K562	blood:
6	chr6:34107259..34108884-chr6:34110412..34112851,2	MCF-7	breast:
7	chr6:34023393..34025806-chr6:34111046..34114201,3	MCF-7	breast:
8	chr6:33677651..33679939-chr6:34111673..34114600,2	MCF-7	breast:
9	chr6:34023163..34023796-chr6:34111451..34112193,2	MCF-7	breast:
10	chr6:34101607..34103904-chr6:34110827..34112823,3	K562	blood:
11	chr6:34100230..34104042-chr6:34111323..34114936,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000137288	chromatin interactions
ENSG00000124493	chromatin interactions

Extended variants
information (count: 86 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:86 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75432840	chr6:34110808-34110809	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs148780119	chr6:34110823-34110824	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142559507	chr6:34110824-34110825	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375692661	chr6:34110850-34110851	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs2026490	chr6:34110880-34110881	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs182126021	chr6:34110887-34110888	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150970591	chr6:34110892-34110893	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs185915785	chr6:34110918-34110919	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189267334	chr6:34110919-34110920	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528746244	chr6:34110971-34110972	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554088698	chr6:34110987-34110988	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181192913	chr6:34110993-34110994	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs2451332	chr6:34110996-34110997	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs568644300	chr6:34111001-34111002	Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs79037435	chr6:34111004-34111005	Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs78907911	chr6:34111061-34111062	Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs185844360	chr6:34111139-34111140	Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs190610963	chr6:34111140-34111141	Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs577420117	chr6:34111141-34111142	Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs371381749	chr6:34111156-34111157	Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs183197314	chr6:34111163-34111164	Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs375455428	chr6:34111189-34111190	Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs144159282	chr6:34111196-34111197	Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs11755375	chr6:34111207-34111208	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs541554413	chr6:34111242-34111243	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs563043158	chr6:34111244-34111245	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs115926387	chr6:34111257-34111258	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs527712702	chr6:34111278-34111279	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs573069700	chr6:34111281-34111282	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs530660860	chr6:34111311-34111312	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs186108500	chr6:34111372-34111373	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs564226830	chr6:34111433-34111434	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs192127484	chr6:34111441-34111442	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs113847202	chr6:34111450-34111451	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs147775935	chr6:34111472-34111473	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs59829177	chr6:34111479-34111480	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs371687952	chr6:34111484-34111485	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs570124018	chr6:34111487-34111488	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs374663919	chr6:34111495-34111496	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs537250083	chr6:34111780-34111781	Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs559077699	chr6:34111797-34111798	Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs577479711	chr6:34111811-34111812	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs573486194	chr6:34111827-34111828	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs376132420	chr6:34111833-34111834	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs574143870	chr6:34111871-34111872	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs543944354	chr6:34111880-34111881	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs369437013	chr6:34111896-34111897	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs183951159	chr6:34111903-34111904	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs545702402	chr6:34111940-34111941	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs371544274	chr6:34111942-34111943	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
Acute myeloid leukemia	20729466	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
Esophageal adenocarcinoma	18820669	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
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:430 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34104400-34111400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr6:34107600-34111400	Weak transcription	Right Atrium	heart
3	chr6:34108400-34111400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
4	chr6:34108400-34111600	Bivalent Enhancer	Fetal Muscle Leg	muscle
5	chr6:34109600-34111400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
6	chr6:34109600-34111400	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
7	chr6:34109600-34111400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
8	chr6:34109600-34111400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
9	chr6:34109600-34111600	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr6:34109800-34111200	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
11	chr6:34109800-34111400	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
12	chr6:34109800-34111600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
13	chr6:34110000-34111400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr6:34110000-34111400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
15	chr6:34110000-34111800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr6:34110000-34111800	Enhancers	Spleen	Spleen
17	chr6:34110000-34112600	Bivalent Enhancer	Fetal Brain Male	brain
18	chr6:34110000-34112600	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
19	chr6:34110200-34110800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
20	chr6:34110200-34111400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr6:34110200-34111400	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
22	chr6:34110200-34111400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr6:34110200-34111400	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
24	chr6:34110200-34111600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
25	chr6:34110200-34111600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
26	chr6:34110200-34111600	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
27	chr6:34110200-34111800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr6:34110200-34111800	Bivalent Enhancer	Fetal Stomach	stomach
29	chr6:34110200-34113200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
30	chr6:34110200-34114000	Bivalent Enhancer	Placenta	Placenta
31	chr6:34110400-34110800	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
32	chr6:34110400-34110800	Bivalent Enhancer	Primary T cells from cord blood	blood
33	chr6:34110400-34110800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr6:34110400-34110800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr6:34110400-34110800	Enhancers	Gastric	stomach
36	chr6:34110400-34111000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
37	chr6:34110400-34111400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
38	chr6:34110400-34111400	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr6:34110400-34111400	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
40	chr6:34110400-34111600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr6:34110400-34111600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
42	chr6:34110400-34111600	Bivalent Enhancer	Colonic Mucosa	Colon
43	chr6:34110400-34112800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
44	chr6:34110400-34114000	Bivalent Enhancer	Fetal Thymus	thymus
45	chr6:34110600-34110800	Flanking Active TSS	H9 Cell Line	embryonic stem cell
46	chr6:34110600-34110800	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr6:34110600-34110800	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr6:34110600-34110800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
49	chr6:34110600-34110800	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
50	chr6:34110600-34111000	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell

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