Variant report

Variant	esv2758267
Chromosome Location	chr11:48303671-48856977
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1968)
CpG islands
(count:672)
Chromatin interactive
region (count:6)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1968 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:48600198-48600306	K562	blood:	n/a	n/a
2	ATF1	chr11:48845364-48845733	K562	blood:	n/a	n/a
3	ATF1	chr11:48356437-48356637	K562	blood:	n/a	n/a
4	ATF1	chr11:48796111-48796444	K562	blood:	n/a	n/a
5	ATF1	chr11:48849264-48849333	K562	blood:	n/a	n/a
6	ATF3	chr11:48845439-48845653	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr11:48814467-48814498	K562	blood:	n/a	n/a
8	BACH1	chr11:48356973-48356986	K562	blood:	n/a	n/a
9	BATF	chr11:48844167-48844436	GM12878	blood:	n/a	n/a
10	BATF	chr11:48776576-48776723	GM12878	blood:	n/a	n/a
11	BATF	chr11:48831050-48831447	GM12878	blood:	n/a	n/a
12	BATF	chr11:48856700-48857102	GM12878	blood:	n/a	n/a
13	BATF	chr11:48834286-48834608	GM12878	blood:	n/a	n/a
14	BATF	chr11:48839569-48839852	GM12878	blood:	n/a	n/a
15	BATF	chr11:48854717-48855191	GM12878	blood:	n/a	n/a
16	BATF	chr11:48805015-48805320	GM12878	blood:	n/a	n/a
17	BATF	chr11:48817733-48818014	GM12878	blood:	n/a	n/a
18	BATF	chr11:48775367-48775560	GM12878	blood:	n/a	n/a
19	BATF	chr11:48854637-48855193	GM12878	blood:	n/a	n/a
20	BATF	chr11:48834403-48834545	GM12878	blood:	n/a	n/a
21	BATF	chr11:48828245-48828541	GM12878	blood:	n/a	n/a
22	BATF	chr11:48844232-48844479	GM12878	blood:	n/a	n/a
23	BATF	chr11:48844664-48844887	GM12878	blood:	n/a	n/a
24	BATF	chr11:48810469-48810756	GM12878	blood:	n/a	n/a
25	BATF	chr11:48776572-48776725	GM12878	blood:	n/a	n/a
26	BATF	chr11:48741581-48741798	GM12878	blood:	n/a	n/a
27	BATF	chr11:48842846-48843034	GM12878	blood:	n/a	n/a
28	BATF	chr11:48810099-48810738	GM12878	blood:	n/a	n/a
29	BATF	chr11:48810174-48810367	GM12878	blood:	n/a	n/a
30	BATF	chr11:48828245-48828584	GM12878	blood:	n/a	n/a
31	BATF	chr11:48856704-48856991	GM12878	blood:	n/a	n/a
32	BATF	chr11:48775372-48775512	GM12878	blood:	n/a	n/a
33	BATF	chr11:48804986-48805223	GM12878	blood:	n/a	n/a
34	BCL11A	chr11:48845478-48845589	H1-hESC	embryonic stem cell:	n/a	n/a
35	BCL11A	chr11:48817850-48818014	GM12878	blood:	n/a	n/a
36	BCL11A	chr11:48854649-48855017	GM12878	blood:	n/a	n/a
37	BCL11A	chr11:48810501-48810790	GM12878	blood:	n/a	n/a
38	BCL11A	chr11:48804969-48805215	GM12878	blood:	n/a	n/a
39	BCL11A	chr11:48831065-48831468	GM12878	blood:	n/a	n/a
40	BCL11A	chr11:48817821-48818049	GM12878	blood:	n/a	n/a
41	BCL11A	chr11:48804912-48805331	GM12878	blood:	n/a	n/a
42	BCL11A	chr11:48775336-48775585	GM12878	blood:	n/a	n/a
43	BCL11A	chr11:48856730-48856963	GM12878	blood:	n/a	n/a
44	BCL11A	chr11:48834381-48834593	GM12878	blood:	n/a	n/a
45	BCL11A	chr11:48845411-48845640	GM12878	blood:	n/a	n/a
46	BCL11A	chr11:48844230-48844427	GM12878	blood:	n/a	n/a
47	BCL11A	chr11:48776528-48776717	GM12878	blood:	n/a	n/a
48	BCL11A	chr11:48843199-48843455	GM12878	blood:	n/a	n/a
49	BCL11A	chr11:48834409-48834539	GM12878	blood:	n/a	n/a
50	BCL11A	chr11:48844176-48844483	GM12878	blood:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48346680-48346730	AG10803	skin:	n/a
2	chr11:48346680-48346730	AG10803	skin:	n/a
3	chr11:48510647-48510697	NT2-D1	testis:	n/a
4	chr11:48345815-48345865	AG09309	skin:	n/a
5	chr11:48346680-48346730	Caco-2	colon:	n/a
6	chr11:48345361-48345411	Caco-2	colon:	n/a
7	chr11:48509488-48509538	HRPEpiC	eye:	n/a
8	chr11:48326388-48326438	SK-N-SH_RA	brain:	n/a
9	chr11:48327164-48327214	BJ	skin:	n/a
10	chr11:48345815-48345865	PANC-1	pancreas:	n/a
11	chr11:48509778-48509828	NHBE	bronchial:	n/a
12	chr11:48509488-48509538	SAEC	small airway:	n/a
13	chr11:48326388-48326438	LNCaP	prostate:	n/a
14	chr11:48345815-48345865	ovcar-3	ovarian:	n/a
15	chr11:48345815-48345865	HCT-116	colon:	n/a
16	chr11:48346680-48346730	HMEC	breast:	n/a
17	chr11:48509778-48509828	GM06990	blood:	n/a
18	chr11:48509778-48509828	A549	lung:	n/a
19	chr11:48328132-48328182	A549	lung:	n/a
20	chr11:48510647-48510697	HCF	heart:	n/a
21	chr11:48346680-48346730	Jurkat	blood:	n/a
22	chr11:48345815-48345865	HEK293	kidney:	embryo
23	chr11:48374446-48374496	HEEpiC	esophagus:	n/a
24	chr11:48345361-48345411	SKMC	muscle:	n/a
25	chr11:48509488-48509538	HCF	heart:	n/a
26	chr11:48346680-48346730	AG09309	skin:	n/a
27	chr11:48374446-48374496	IMR90	lung:	fetal
28	chr11:48326388-48326438	AG09319	gingival:	n/a
29	chr11:48367974-48368024	GM19239	blood:	n/a
30	chr11:48509778-48509828	SK-N-SH	brain:	n/a
31	chr11:48367974-48368024	HPAEpiC	pulmonary alveolar:	n/a
32	chr11:48327164-48327214	SK-N-SH	brain:	n/a
33	chr11:48345815-48345865	GM12878	blood:	n/a
34	chr11:48367974-48368024	LNCaP	prostate:	n/a
35	chr11:48367974-48368024	PANC-1	pancreas:	n/a
36	chr11:48367974-48368024	GM06990	blood:	n/a
37	chr11:48326388-48326438	HEK293	kidney:	embryo
38	chr11:48374446-48374496	Caco-2	colon:	n/a
39	chr11:48326388-48326438	AG10803	skin:	n/a
40	chr11:48345815-48345865	HCF	heart:	n/a
41	chr11:48509778-48509828	HEK293	kidney:	embryo
42	chr11:48345815-48345865	HAEpiC	amniotic membrane:	n/a
43	chr11:48374446-48374496	GM12892	blood:	n/a
44	chr11:48346680-48346730	BJ	skin:	n/a
45	chr11:48345815-48345865	PrEC	prostate:	n/a
46	chr11:48345815-48345865	T-47D	breast:	n/a
47	chr11:48345815-48345865	Jurkat	blood:	n/a
48	chr11:48367974-48368024	NH-A	brain:	n/a
49	chr11:48367974-48368024	SK-N-SH_RA	brain:	n/a
50	chr11:48345361-48345411	IMR90	lung:	fetal

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:48366878..48368914-chr11:48372533..48375413,2	MCF-7	breast:
2	chr11:48478071..48478587-chr11:49191267..49191777,2	MCF-7	breast:
3	chr11:48361908..48364233-chr11:48365831..48368223,2	MCF-7	breast:
4	chr11:48234220..48234962-chr11:48329425..48329937,2	MCF-7	breast:
5	chr11:48811378..48811898-chr8:46850618..46851141,2	MCF-7	breast:
6	chr11:48361908..48364233-chr11:48365831..48368223,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4C5-1	chr11:48507915-48508377	NONHSAT021297

No data

Variant related genes	Relation type
OR4C9P	TF binding region
OR4C10P	TF binding region
OR4A47	TF binding region
OR4C2P	TF binding region
OR4A41P	TF binding region
OR4A46P	TF binding region
OR4A45P	TF binding region
OR4R1P	TF binding region
OR4A43P	TF binding region
OR4C5	TF binding region
OR4C4P	TF binding region
OR4A40P	TF binding region
OR4A44P	TF binding region
OR4A48P	TF binding region
OR4C3	TF binding region
OR4S1	TF binding region
OR4A42P	TF binding region
OR4C9P	CpG island
OR4C10P	CpG island
OR4A47	CpG island
OR4C2P	CpG island
OR4A41P	CpG island
OR4A46P	CpG island
OR4A45P	CpG island
OR4R1P	CpG island
OR4A43P	CpG island
OR4C5	CpG island
OR4C4P	CpG island
OR4A40P	CpG island
OR4A44P	CpG island
OR4A48P	CpG island
OR4C3	CpG island
OR4S1	CpG island
OR4A42P	CpG island
ENSG00000197161	chromatin interactions

Extended variants
information (count: 15566 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:15566 , 50 per page) page: 1 2 3 4 5 6 7 ... 312

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138705662	chr11:48314014-48314015	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs188141748	chr11:48314023-48314024	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs114745544	chr11:48314061-48314062	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs12146571	chr11:48314077-48314078	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs542154898	chr11:48314089-48314090	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs562039272	chr11:48314090-48314091	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs10838862	chr11:48314105-48314106	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs35538759	chr11:48314133-48314134	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs145048026	chr11:48314134-48314135	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs541599301	chr11:48314144-48314145	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs537174767	chr11:48314148-48314149	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs533439753	chr11:48314149-48314150	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs549913508	chr11:48314162-48314163	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs141062053	chr11:48314163-48314164	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs535428087	chr11:48314224-48314225	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs10838863	chr11:48314225-48314226	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs548550936	chr11:48314242-48314243	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs190340114	chr11:48314246-48314247	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs148510576	chr11:48314284-48314285	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs547539952	chr11:48314296-48314297	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs368950026	chr11:48314310-48314311	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs11039644	chr11:48314317-48314318	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs536897812	chr11:48314332-48314333	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs151069291	chr11:48314343-48314344	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs555974047	chr11:48314344-48314345	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs76551791	chr11:48314361-48314362	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs535059400	chr11:48314362-48314363	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs78169865	chr11:48326395-48326396	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs139509706	chr11:48326415-48326416	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs528670448	chr11:48326848-48326849	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs546757604	chr11:48326873-48326874	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs529428519	chr11:48326875-48326876	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs146880199	chr11:48326888-48326889	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs570414118	chr11:48326904-48326905	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs183834662	chr11:48326959-48326960	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs7130032	chr11:48326963-48326964	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs570195676	chr11:48327029-48327030	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs189100425	chr11:48327043-48327044	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs75301774	chr11:48327057-48327058	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs555901913	chr11:48327164-48327165	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs566150547	chr11:48327165-48327166	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs1483122	chr11:48327186-48327187	Inactive region	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs140748221	chr11:48327213-48327214	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
44	rs189030604	chr11:48327772-48327773	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs371797596	chr11:48328011-48328012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs376510610	chr11:48328016-48328017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs78420375	chr11:48328027-48328028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs138486462	chr11:48328029-48328030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs143021148	chr11:48328042-48328043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs146061383	chr11:48328046-48328047	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Breast cancer	21990379	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Schizophrenia	20967226	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Medulloblastoma	21163964	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Intellectual disability	22045946	CNVD

Chromatin state (count:410 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48314000-48314400	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr11:48328000-48328400	Enhancers	Lung	lung
3	chr11:48329400-48329800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
4	chr11:48329400-48330000	Enhancers	Primary T helper cells fromperipheralblood	blood
5	chr11:48329600-48329800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
6	chr11:48329600-48329800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr11:48329600-48329800	Enhancers	Brain Angular Gyrus	brain
8	chr11:48329600-48329800	Enhancers	Brain Cingulate Gyrus	brain
9	chr11:48329600-48329800	Enhancers	Brain Hippocampus Middle	brain
10	chr11:48336400-48337600	Enhancers	Stomach Mucosa	stomach
11	chr11:48337600-48341200	Weak transcription	Stomach Mucosa	stomach
12	chr11:48341200-48342600	Enhancers	Stomach Mucosa	stomach
13	chr11:48341400-48345800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
14	chr11:48341600-48341800	Bivalent Enhancer	Left Ventricle	heart
15	chr11:48341600-48342000	Bivalent Enhancer	Right Atrium	heart
16	chr11:48341600-48342000	Enhancers	Spleen	Spleen
17	chr11:48341800-48342000	Enhancers	Left Ventricle	heart
18	chr11:48342600-48344400	Weak transcription	Stomach Mucosa	stomach
19	chr11:48344400-48344800	Enhancers	Stomach Mucosa	stomach
20	chr11:48344800-48349800	Weak transcription	Stomach Mucosa	stomach
21	chr11:48346600-48346800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr11:48346600-48347000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
23	chr11:48346600-48347400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr11:48346600-48348600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
25	chr11:48346800-48347400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr11:48348800-48350000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr11:48350000-48355600	Weak transcription	Stomach Mucosa	stomach
28	chr11:48352400-48353400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
29	chr11:48352400-48353800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
30	chr11:48353000-48359800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
31	chr11:48355200-48363800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr11:48355600-48357000	Enhancers	Stomach Mucosa	stomach
33	chr11:48357000-48358000	Weak transcription	Stomach Mucosa	stomach
34	chr11:48358000-48358200	Enhancers	Stomach Mucosa	stomach
35	chr11:48362000-48362200	Enhancers	Primary T helper naive cells from peripheral blood	blood
36	chr11:48362400-48362800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr11:48362800-48363200	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr11:48362800-48363200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr11:48362800-48363600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
40	chr11:48362800-48363800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
41	chr11:48363000-48363200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
42	chr11:48363000-48363400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
43	chr11:48363000-48363400	Active TSS	A549	lung
44	chr11:48363000-48363600	Active TSS	Hela-S3	cervix
45	chr11:48363000-48363800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
46	chr11:48363000-48363800	Enhancers	Primary T helper cells PMA-I stimulated	--
47	chr11:48363200-48363600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
48	chr11:48363200-48363600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
49	chr11:48363200-48363600	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chr11:48363200-48363600	Enhancers	Primary T killer memory cells from peripheral blood	blood

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