Variant report

Variant	esv3380731
Chromosome Location	chr1:227975029-227977177
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:18)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:227967943..227969824-chr1:227975075..227977321,2	K562	blood:
2	chr1:227962656..227964965-chr1:227972636..227975785,3	MCF-7	breast:
3	chr1:227921116..227924283-chr1:227974450..227977412,3	MCF-7	breast:
4	chr1:227974971..227975949-chr1:228089646..228090423,2	MCF-7	breast:
5	chr1:227974795..227976825-chr1:227979678..227981441,2	MCF-7	breast:
6	chr1:227973508..227976414-chr1:228271906..228274660,2	K562	blood:
7	chr1:227977112..227980203-chr1:227982448..227986232,4	MCF-7	breast:
8	chr1:227970937..227973164-chr1:227974338..227975949,2	K562	blood:
9	chr1:227973847..227976813-chr1:228134403..228136465,4	MCF-7	breast:
10	chr1:227966135..227968360-chr1:227973552..227975937,2	MCF-7	breast:
11	chr1:227973990..227976500-chr1:228134426..228136462,3	MCF-7	breast:
12	chr1:227974881..227977726-chr20:49346280..49347834,2	MCF-7	breast:
13	chr1:227945394..227947244-chr1:227973849..227976801,2	MCF-7	breast:
14	chr1:227960240..227967392-chr1:227972741..227977657,8	K562	blood:
15	chr1:227976724..227980772-chr1:227980865..227984605,4	MCF-7	breast:
16	chr1:227949805..227950774-chr1:227975453..227976341,2	K562	blood:
17	chr1:227963946..227966853-chr1:227977108..227980456,3	MCF-7	breast:
18	chr1:227970651..227973164-chr1:227973342..227975838,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNAP47-1	chr1:227975396-227975712	NONHSAT009948
2	lnc-SNAP47-1	chr1:227976849-227977741	NONHSAT009948
3	lnc-SNAP47-1	chr1:227975807-227979880	NONHSAT009949

No data

Variant related genes	Relation type
ENSG00000143816	chromatin interactions
ENSG00000143740	chromatin interactions
ENSG00000081692	chromatin interactions

Extended variants
information (count: 70 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:70 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568328949	chr1:227975058-227975059	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs529186624	chr1:227975136-227975137	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs142547487	chr1:227975147-227975148	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs370492403	chr1:227975148-227975149	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs373608475	chr1:227975154-227975155	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs117977156	chr1:227975249-227975250	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs557529540	chr1:227975269-227975270	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs566467719	chr1:227975274-227975275	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs370379326	chr1:227975295-227975296	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs150513352	chr1:227975300-227975301	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs553266069	chr1:227975314-227975315	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs60255904	chr1:227975414-227975415	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs535723634	chr1:227975525-227975526	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
14	rs557578639	chr1:227975542-227975543	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
15	rs575739352	chr1:227975576-227975577	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
16	rs76488127	chr1:227975587-227975588	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
17	rs543156557	chr1:227975657-227975658	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
18	rs546287478	chr1:227975675-227975676	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
19	rs561311977	chr1:227975779-227975780	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs564397467	chr1:227975809-227975810	Bivalent/Poised TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
21	rs34752445	chr1:227975811-227975812	Bivalent/Poised TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
22	rs573291750	chr1:227975823-227975824	Bivalent/Poised TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
23	rs35898137	chr1:227975840-227975841	Bivalent/Poised TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
24	rs184218271	chr1:227975849-227975850	Bivalent/Poised TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
25	rs540665519	chr1:227975896-227975897	Bivalent/Poised TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
26	rs562041619	chr1:227975902-227975903	Bivalent/Poised TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
27	rs529253891	chr1:227975912-227975913	Bivalent/Poised TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
28	rs188844739	chr1:227976021-227976022	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
29	rs140253371	chr1:227976148-227976149	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
30	rs532938890	chr1:227976166-227976167	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
31	rs371881433	chr1:227976263-227976264	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
32	rs191777439	chr1:227976276-227976277	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
33	rs566194209	chr1:227976291-227976292	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
34	rs533624796	chr1:227976292-227976293	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
35	rs548594346	chr1:227976306-227976307	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
36	rs184582687	chr1:227976309-227976310	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
37	rs189102981	chr1:227976330-227976331	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
38	rs200451667	chr1:227976399-227976400	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
39	rs374371023	chr1:227976415-227976416	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
40	rs144519274	chr1:227976420-227976421	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
41	rs540486284	chr1:227976429-227976430	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
42	rs558316942	chr1:227976443-227976444	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
43	rs573403232	chr1:227976453-227976454	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
44	rs540728336	chr1:227976467-227976468	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
45	rs562107715	chr1:227976479-227976480	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
46	rs10799449	chr1:227976498-227976499	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs544499291	chr1:227976534-227976535	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
48	rs562615351	chr1:227976548-227976549	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
49	rs182439094	chr1:227976554-227976555	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
50	rs147849117	chr1:227976584-227976585	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:473 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:227955800-227975200	Weak transcription	Hela-S3	cervix
2	chr1:227958000-227975200	Weak transcription	A549	lung
3	chr1:227970600-227975400	Weak transcription	K562	blood
4	chr1:227973400-227975200	Bivalent Enhancer	Fetal Thymus	thymus
5	chr1:227973600-227975800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
6	chr1:227973600-227975800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
7	chr1:227974000-227975200	Flanking Active TSS	Rectal Smooth Muscle	rectum
8	chr1:227974000-227975200	Enhancers	Sigmoid Colon	Sigmoid Colon
9	chr1:227974000-227975400	Flanking Active TSS	Stomach Smooth Muscle	stomach
10	chr1:227974200-227975200	Enhancers	Small Intestine	intestine
11	chr1:227974400-227975200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr1:227974400-227975200	Flanking Active TSS	Brain Anterior Caudate	brain
13	chr1:227974400-227975200	Flanking Active TSS	Colon Smooth Muscle	Colon
14	chr1:227974400-227975200	Flanking Active TSS	Pancreas	Pancrea
15	chr1:227974400-227975600	Flanking Active TSS	Duodenum Mucosa	Duodenum
16	chr1:227974400-227975600	Flanking Bivalent TSS/Enh	HepG2	liver
17	chr1:227974600-227975200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr1:227974600-227975200	Flanking Bivalent TSS/Enh	Muscle Satellite Cultured Cells	--
19	chr1:227974600-227975200	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr1:227974600-227975200	Flanking Active TSS	Gastric	stomach
21	chr1:227974600-227975200	Flanking Active TSS	Ovary	ovary
22	chr1:227974600-227975400	Flanking Active TSS	Brain Cingulate Gyrus	brain
23	chr1:227974600-227975600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr1:227974600-227975600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
25	chr1:227974600-227975600	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
26	chr1:227974600-227975800	Flanking Active TSS	Adipose Nuclei	Adipose
27	chr1:227974600-227977000	Active TSS	Pancreatic Islets	Pancreatic Islet
28	chr1:227974800-227975200	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
29	chr1:227974800-227975200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
30	chr1:227974800-227975200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr1:227974800-227975200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
32	chr1:227974800-227975200	Flanking Active TSS	Brain Angular Gyrus	brain
33	chr1:227974800-227975200	Flanking Active TSS	Brain Hippocampus Middle	brain
34	chr1:227974800-227975200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
35	chr1:227974800-227975200	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
36	chr1:227974800-227975200	Flanking Bivalent TSS/Enh	Fetal Lung	lung
37	chr1:227974800-227975200	Flanking Active TSS	Left Ventricle	heart
38	chr1:227974800-227975200	Flanking Active TSS	Psoas Muscle	Psoas
39	chr1:227974800-227975200	Flanking Active TSS	Right Ventricle	heart
40	chr1:227974800-227975200	Flanking Active TSS	GM12878-XiMat	blood
41	chr1:227974800-227975200	Flanking Active TSS	NHDF-Ad	bronchial
42	chr1:227974800-227975200	Flanking Active TSS	NHLF	lung
43	chr1:227974800-227975400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr1:227974800-227975400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr1:227974800-227975400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
46	chr1:227974800-227975400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr1:227974800-227975400	Flanking Active TSS	Fetal Heart	heart
48	chr1:227974800-227975400	Flanking Active TSS	Spleen	Spleen
49	chr1:227974800-227975600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr1:227974800-227975600	Flanking Active TSS	Primary T cells from cord blood	blood

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